The concurrence of ring constrictions in Adams-Oliver syndrome: Additional evidence for vascular disruption as common pathogenetic mechanism

Genetic Counseling

Volumn 10, Issue 3, 1999, Pages 295-300

  Keymolen, K ^c   De Smet, L ^c   Bracke, P ^a   Fryns, J P ^b  

^a Paediatrician   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

^c NONE

Author keywords

Adams Oliver syndrome; Autosomal dominant inheritance; Ring constrictions; Vascular disruption

Indexed keywords

ADAMS OLIVER SYNDROME; AMNION BAND; ARTICLE; CASE REPORT; CHILD; FEMALE; HUMAN; INFANT; LIMB DEFECT; NEWBORN; PATHOGENESIS; SCALP; SKIN DEFECT; VASCULAR DISEASE; VASOCONSTRICTION;

ABNORMALITIES, MULTIPLE; BRAIN DISEASES; CONSTRICTION, PATHOLOGIC; CYSTS; FACE; FEMALE; FINGERS; FOOT DEFORMITIES, CONGENITAL; GENES, DOMINANT; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT; SCALP; SYNDROME; TOES;

EID: 0032844582     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. ADAMS F.H., OLIVER C.P.: Hereditary deformities in man due to arrested development. J. Hered., 1945, 36, 3-7.
2. BAMFORTH J.S., KAURAH P., BYRNE J., FERREIRA P.: Adams Oliver syndrome: A family with extreme variability in clinical expression. Am. J. Med. Genet., 1994, 49, 393-396.
3. CHABROLLE J.P., LESAGE B., ROSIER A.: Aplasia cutanéo-osseuse du scalp avec anomalie des extremités. Ann. Pediatr., 1975, 22, 613-618.
4. DER KALOUSTIAN V.M., HOYME H.E., HOGG H., ENTIN M.A., GUTTMACHER A.E.: Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome. Am. J. Med. Genet., 1991, 38, 69-73.
5. FARMER A.W., MAXMEN M.D.: Congenital absence of the skin. Plast. Reconstr. Surg., 1960, 25, 435-440.
6. FRYNS J.P.: Congenital scalp defects with distal limb reduction anomalies. J. Med. Genet., 1987, 24, 493-496.
7. FRYNS J.P., LEGIUS E., DEMAEREL P., VAN DEN BERGHE H.: Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media. Clin. Genet., 1996, 50, 505-509.
8. HILL L.M., KISLAK S., JONES N.: Prenatal ultrasound diagnosis of a forearm constriction band. J Ultrasound Med. 1988, 7, 293-295.
9. HOYME H., JONES K.L., VAN ALLEN M.I., SAUNDERS B.S., BENIRSCHKE K.: Vascular pathogenesis of transverse limb reduction defects. J. Pediatr., 1982, 101, 839-843.
10. IRONS G.B., OLSON R.M.: Aplasia cutis congenita. Plast. Reconstr. Surg., 1980, 66, 199-203.
11. JAEGGI E., KIND C., MORGER R.: Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of three additional cases. Eur. J. Pediatr., 1990, 149, 565-566.
12. KOIFFMANN C.P., WAJNTAL A., HUYKE B.J., CASTRO R.M.: Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome -McKusick 10030): further evidence of autosomal recessive inheritance. Am. J. Med. Genet., 1988, 29, 263-268.
13. MOERMAN P., FRYNS J.P., VANDENBERGHE K., LAUWERYNS J.: Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlap. Am. J. Med. Genet., 1992, 42, 470-479.
14. ÖRSTAVIK K.H., STRÖMME P., SPETALEN S., FLAGE T., WESTVIK J., VESTERHUS P., SKJELDAL O.: Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome? Am. J. Med. Genet., 1995, 59, 92-95.
15. POUSTI T.J., BARTLETT R.A.: Adams-Oliver syndrome: genetics and associated anomalies of cutis aplasia. Plast. Reconstr. Surg., 1997, 100, 1491-1496.
16. SCRIBANU N., TENTAMY S.A.: The syndrome of apiasia cutis congenita with terminal transverse defects of the limbs. J Pediatr., 1975, 87, 79-82.
17. STEPHAN M.J., SMITH D.W., PONZI J.W., ALDEN E.R.: Origin of scalp vertex aplasia cutis. J. Pediatr., 1982, 101, 850-853.
18. SYBERT V.P.: Aplasia cutis congenita: a report of 12 new families and review of the literature. Pediatr. Dermatol., 1985, 3, 1-14.
19. TORIELLO H.V., GRAFF R.G., FLORENTINE M.F., LACINA S., MOORE W.D.: Scalp and limb defects with cutis marmorata telengiectatica congenita: Adams-Oliver syndrome? Am. J. Med. Genet., 1988, 29, 269-276.
20. VAN ALLEN M.I.: Structural anomalies resulting from vascular disruption. Ped. Clin. North Am., 1992, 39, 255-277.
21. VAN ALLEN M.I., CURRY C., CALLAGHER L.: Limb body wall complex: 1. Pathogenesis. Am. J. Med. Genet., 1987, 28, 529-548.
22. VAN ALLEN M.I., MYHRE S.: Ectopia cordis thoracalis with craniofacial defects resulting from early amnion rupture. Teratology, 1985, 32, 19-24.
23. VAN ALLEN M.I., SIEGEL-BARTELT J., DIXON J., ZUKER R.M., CLARKE H.M., TOI A.: Constriction bands and limb reduction defects in two newborns with fetal ultrasound evidence for vascular disruption. Am. J. Med. Genet., 1992, 44, 598-604.
24. WHITLEY C.B., GORLIN R.J.: Adams-Oliver syndrome revisited. Am. J. Med. Genet., 1991, 40, 319-326.
25. ZAPATA H.H., SLETTEN L.J., PIERPONT M.E.M.: Congenital cardiac malformations in Adams-Oliver syndrome. Clin. Genet., 1995, 47, 80-84.